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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 472생성일: 2026년 10월 23일

4-Aminomethyltetrahydropyran → 3-Bromo-4-methoxy-N-[(oxan-4-yl)methyl]aniline

https://huagongshe.com/ko/reaction/472

반응식

참여 물질

역할이름HCID투입량
반응물4-AminomethyltetrahydropyranHCID 2773210—
반응물2-Bromo-4-iodoanisoleHCID 3376779—
시약Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
촉매Palladium (II) acetateHCID 4144353—
용매1,4-DioxaneHCID 31275—
생성물3-Bromo-4-methoxy-N-[(oxan-4-yl)methyl]anilineHCID 655102420%

반응 조건

온도80 °C

반응 단계

Palladium (II) acetate (0.075 g, 0.34 mmol) and racemic-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (0.223 g, 0.36 mmol) were suspended in dioxane (5mL). The mixture was evacuated and purged with nitrogen, and warmed to 50°C. In a separate vessel, 2-bromo-4-iodo-1-methoxybenzene (1.4 g, 4.47 mmol), (tetrahydro-2H-pyran-4-yl)methanamine (0.547 mL, 4.47 mmol) and sodium-t- butoxide (0.645 g, 6.71 mmol) were suspended in dioxane (5ML). The resulting mixture was evacuated, purged with nitrogen and warmed to 50°C. After ~30 mins, the catalyst mixture was transferred to the reaction vessel. The reaction was evacuated and purged with nitrogen and heated at 80°C overnight. Very little product and mainly SM so reaction abandoned.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-6117c2ee846f49c3a77484ecf172e880
출처 메모750 AstraZeneca ELN dataset